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Efficacy of Repetitive Transcranial Magnetic Stimulation in Adult Attention Deficit Disorder

Not Applicable
Completed
Conditions
ADHD
Attention Deficit Disorder
Interventions
Device: repetitive Transcranial Magnetic Stimulation
Registration Number
NCT06030024
Lead Sponsor
University of Tehran
Brief Summary

The purpose of the current open-lable study was to use low-frequency repetitive transcranial magnetic stimulation (rTMS) to improve the attention deficits in a sample of adult patients suffering from attention deficit disorder. Participants received 10 sessions of rTMS over Fz (located using the EEG 10-20 international system) and underwent assessments of their attentional capacity using the gradCPT task in an fMRI scanner, before and after the intervention. Other behavioral assessments of their attention symptoms have also been conducted.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria
  • Normal intelligence level (>90)
  • Diagnosis of ADD by a psychiatrist using the ADHD-RS-IV with Adult Prompts
Exclusion Criteria
  • Scores of 21 or more on BDI and/or BAI
  • History of head trauma
  • History of a major psychological or neurological condition
  • Presence of metal in the head
  • History of seizures
  • Serious cardiovascular disease
  • Use of medications with an impact on cognitive functions during the treatment window (patients with a constant and stable dose were included)
  • Recent use of alcohol or substance abuse

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Active rTMSrepetitive Transcranial Magnetic StimulationParticipants in this one and only arm in the current study received active repetitive transcranial magnetic stimulation.
Primary Outcome Measures
NameTimeMethod
Change in performanceUp to 10 days, i.e., before and after the completion of the 10 sessions of rTMS

Shortened version (4 min) of the continuous go/no-go task: gradual-onset continuous performance task (gradCPT)

Secondary Outcome Measures
NameTimeMethod
Change in self-report attention scoresBaseline, after 5 days of stimulation, after 10 days of stimulation; Range= 0-6; Higher scores represent worse outcome

The 6-item ASRS-V1.1 Adult ADHD Self-Report

Change in investigator-rated attention scoresBaseline, after 5 days of stimulation, after 10 days of stimulation; Range:0 - 54; Higher scores represent worse outcome

Investigator-Rated Attention-Deficit Hyperactivity Disorder (ADHD) Rating Scale-IV (I-ADHD RS-IV) with adult prompts

Trial Locations

Locations (1)

National Brain Mapping Lab

🇮🇷

Tehran, Iran, Islamic Republic of

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